array:23 [ "pii" => "S2387020619304279" "issn" => "23870206" "doi" => "10.1016/j.medcle.2019.02.029" "estado" => "S300" "fechaPublicacion" => "2019-11-15" "aid" => "4814" "copyright" => "Elsevier España, S.L.U.. All rights reserved" "copyrightAnyo" => "2019" "documento" => "article" "crossmark" => 1 "subdocumento" => "sco" "cita" => "Med Clin. 2019;153:e52" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "Traduccion" => array:1 [ "en" => array:19 [ "pii" => "S002577531930209X" "issn" => "00257753" "doi" => "10.1016/j.medcli.2019.02.023" "estado" => "S300" "fechaPublicacion" => "2019-11-15" "aid" => "4814" "copyright" => "Elsevier España, S.L.U." "documento" => "article" "crossmark" => 1 "subdocumento" => "sco" "cita" => "Med Clin. 2019;153:e52" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 6 "formatos" => array:2 [ "HTML" => 4 "PDF" => 2 ] ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Image in medicine</span>" "titulo" => "Rosai–Dorfman Disease: A rare cause of massive lymphadenopathy" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:1 [ "paginaInicial" => "e52" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Enfermedad de Rosai-Dorfman: una causa rara de linfadenopatía masiva" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:6 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 675 "Ancho" => 900 "Tamanyo" => 214806 ] ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Marta Custódio, Isa Silva, Anabela Salgueiro Marques" "autores" => array:3 [ 0 => array:2 [ "nombre" => "Marta" "apellidos" => "Custódio" ] 1 => array:2 [ "nombre" => "Isa" "apellidos" => "Silva" ] 2 => array:2 [ "nombre" => "Anabela Salgueiro" "apellidos" => "Marques" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S2387020619304279" "doi" => "10.1016/j.medcle.2019.02.029" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2387020619304279?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S002577531930209X?idApp=UINPBA00004N" "url" => "/00257753/0000015300000009/v1_201910300628/S002577531930209X/v1_201910300628/en/main.assets" ] ] "itemAnterior" => array:19 [ "pii" => "S2387020619304383" "issn" => "23870206" "doi" => "10.1016/j.medcle.2019.04.023" "estado" => "S300" "fechaPublicacion" => "2019-11-15" "aid" => "4920" "copyright" => "Elsevier España, S.L.U." "documento" => "simple-article" "crossmark" => 1 "subdocumento" => "cor" "cita" => "Med Clin. 2019;153:e50-e51" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "en" => array:10 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Letter to the Editor</span>" "titulo" => "Reply" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "e50" "paginaFinal" => "e51" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Respuesta" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Laura Rivilla Marugán, Saioa Zalba Marcos, José Antonio García Erce" "autores" => array:3 [ 0 => array:2 [ "nombre" => "Laura" "apellidos" => "Rivilla Marugán" ] 1 => array:2 [ "nombre" => "Saioa" "apellidos" => "Zalba Marcos" ] 2 => array:2 [ "nombre" => "José Antonio" "apellidos" => "García Erce" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0025775319304415" "doi" => "10.1016/j.medcli.2019.04.040" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0025775319304415?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2387020619304383?idApp=UINPBA00004N" "url" => "/23870206/0000015300000009/v1_201911071124/S2387020619304383/v1_201911071124/en/main.assets" ] "en" => array:12 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Image in medicine</span>" "titulo" => "Rosai–Dorfman Disease: A rare cause of massive lymphadenopathy" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:1 [ "paginaInicial" => "e52" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Marta Custódio, Isa Silva, Anabela Salgueiro Marques" "autores" => array:3 [ 0 => array:4 [ "nombre" => "Marta" "apellidos" => "Custódio" "email" => array:1 [ 0 => "martaisabelcustodio@hotmail.com" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:2 [ "nombre" => "Isa" "apellidos" => "Silva" ] 2 => array:2 [ "nombre" => "Anabela Salgueiro" "apellidos" => "Marques" ] ] "afiliaciones" => array:1 [ 0 => array:2 [ "entidad" => "Cascais Hospital, Portugal" "identificador" => "aff0005" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Enfermedad de Rosai-Dorfman: una causa rara de linfadenopatía masiva" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:6 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 675 "Ancho" => 900 "Tamanyo" => 214806 ] ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0010" class="elsevierStylePara elsevierViewall">Forty-year-old black female, with no previous medical history, presented in the Emergency Department complaining about a mass on her neck that she noticed in the previous five days. Physical examination uncovered a large painless left submandibular mass (5<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>cm), with multiple smaller ones bilaterally. Computed tomography showed multiple cervical and mediastinal adenopathies, more exuberantly on the left lateral lymphatic chain (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). Histology revealed macrophages in a background with eosinophils and emperipolesis (phagocytosis of intact lymphocytes and other immune cells by histiocytes) suggesting Rosai–Dorfman Disease (RDD) (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Also known as sinus histiocytosis with massive lymphadenopathy, RDD is an extremely rare disorder of unknown origin, whose diagnosis is histological, characterized by emperipolesis (phagocytosis of intact lymphocytes and other immune cells by histiocytes).</p><p id="par0020" class="elsevierStylePara elsevierViewall">Predominantly appears in the first two decades, with male-to-female ratio of 5:1.</p><p id="par0025" class="elsevierStylePara elsevierViewall">Clinically causes massive painless lymphadenopathies (most cervical), fever (30%) and extra-nodal involvement (40%).</p><p id="par0030" class="elsevierStylePara elsevierViewall">Differential diagnosis includes reactive lymph node hyperplasia, tuberculosis or lymphoma, among others.</p><p id="par0035" class="elsevierStylePara elsevierViewall">Even though a benign self-limiting disease, treatment may be necessary, although still controversial.</p></span>" "pdfFichero" => "main.pdf" "tienePdf" => true "multimedia" => array:2 [ 0 => array:6 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 853 "Ancho" => 900 "Tamanyo" => 47710 ] ] ] 1 => array:6 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 675 "Ancho" => 900 "Tamanyo" => 214806 ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/23870206/0000015300000009/v1_201911071124/S2387020619304279/v1_201911071124/en/main.assets" "Apartado" => array:4 [ "identificador" => "51820" "tipo" => "SECCION" "en" => array:2 [ "titulo" => "Images in medicine" "idiomaDefecto" => true ] "idiomaDefecto" => "en" ] "PDF" => "https://static.elsevier.es/multimedia/23870206/0000015300000009/v1_201911071124/S2387020619304279/v1_201911071124/en/main.pdf?idApp=UINPBA00004N&text.app=https://www.elsevier.es/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2387020619304279?idApp=UINPBA00004N" ]
Journal Information
Vol. 153. Issue 9.
Pages e52 (November 2019)
Vol. 153. Issue 9.
Pages e52 (November 2019)
Image in medicine
Rosai–Dorfman Disease: A rare cause of massive lymphadenopathy
Enfermedad de Rosai-Dorfman: una causa rara de linfadenopatía masiva
Visits
5
Marta Custódio
, Isa Silva, Anabela Salgueiro Marques
Corresponding author
Cascais Hospital, Portugal
This item has received
Article information
These are the options to access the full texts of the publication Medicina Clínica (English Edition)
Subscriber
Subscribe
Purchase
Contact
Phone for subscriptions and reporting of errors
From Monday to Friday from 9 a.m. to 6 p.m. (GMT + 1) except for the months of July and August which will be from 9 a.m. to 3 p.m.
Calls from Spain
932 415 960
Calls from outside Spain
+34 932 415 960
E-mail